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Adaptive Servoventilation for Treatment of Sleep-Disordered Breathing in Heart Failure A Systematic Review and Meta-analysis

Journal

CHEST
Volume 142, Issue 5, Pages 1211-1221

Publisher

ELSEVIER
DOI: 10.1378/chest.12-0815

Keywords

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Funding

  1. American Heart Association (AHA) [11POST5660004]
  2. US National Institutes of Health [5R01HL085188-04, 5R0HL090897-03, 5K24HL093218-03, 1P01HL095491-01A1]
  3. AHA [0840159N]
  4. Philips Respironics

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Background: Adaptive servoventilation (ASV) has demonstrated efficacy in treating sleep-disordered breathing (SDB) in patients with heart failure (HF), but large randomized trials are lacking. We, therefore, sought to perform a systematic review and meta-analysis of existing data. Methods: A systematic search of the PubMed database was undertaken in March 2012. Publications were independently assessed by two investigators to identify studies of >= 1-week duration that compared ASV to a control condition (ie, subtherapeutic ASV, continuous or bilevel pressure ventilation, oxygen therapy, or no treatment) in adult patients with SDB and HF. Mean, variability, and sample size data were extracted independently for the following outcomes: apneahypopnea index (AHI), left ventricular ejection fraction (LVEF), quality of life (SF-36 Health Survey; Medical Outcomes Trust), 6-min walk distance, peak oxygen consumption ((V)over dotO(2)) % predicted, and ventilatory equivalent ratio for CO2 ((V)over dot(E)/(V)over dotCO(2)) slope measured during exercise. Random effects meta-analysis models were applied. Results: Fourteen studies were identified (N = 538). Comparing ASV to control conditions, the weighted mean difference in AHI (-14.64 events/h; 95% CI, -21.03 to -8.25) and LVEF (0.40; 95% CI, 0.08-0.71) both significantly favored ASV. ASV also improved the 6-min walk distance, but not peak (V)over dotO(2) % predicted, (V)over dot(E)/(V)over dotCO(2) slope, or quality of life, compared with control conditions. Conclusions: In patients with HF and SDB, ASV was more effective than control conditions in reducing the AHI and improving cardiac function and exercise capacity. These data provide a compelling rationale for large-scale randomized controlled trials to assess the clinical impact of ASV on hard outcomes in these patients. CHEST 2012; 142(5):1211-422.1

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